rs9267665
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9267665(C;C) |
Make rs9267665(C;T) |
Make rs9267665(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31903079 |
Gene | C2, ZBTB12 |
is a | snp |
is | mentioned by |
dbSNP | rs9267665 |
dbSNP (classic) | rs9267665 |
ClinGen | rs9267665 |
ebi | rs9267665 |
HLI | rs9267665 |
Exac | rs9267665 |
Gnomad | rs9267665 |
Varsome | rs9267665 |
LitVar | rs9267665 |
Map | rs9267665 |
PheGenI | rs9267665 |
Biobank | rs9267665 |
1000 genomes | rs9267665 |
hgdp | rs9267665 |
ensembl | rs9267665 |
geneview | rs9267665 |
scholar | rs9267665 |
rs9267665 | |
pharmgkb | rs9267665 |
gwascentral | rs9267665 |
openSNP | rs9267665 |
23andMe | rs9267665 |
SNPshot | rs9267665 |
SNPdbe | rs9267665 |
MSV3d | rs9267665 |
GWAS Ctlg | rs9267665 |
GMAF | 0.07622 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21764829] |
Trait | |
Title | A genome-wide association study of hepatitis B vaccine response in an Indonesian population reveals multiple independent risk variants in the HLA region. |
Risk Allele | |
P-val | 1E-17 |
Odds Ratio | 2.0500 [1.64-2.57] |
[PMID 29283494] Genetic association of complement component 2 variants with chronic hepatitis B in a Korean population.